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Items: 4


Inactivating mutations in Drosha mediate vascular abnormalities similar to hereditary hemorrhagic telangiectasia.

Jiang X, Wooderchak-Donahue WL, McDonald J, Ghatpande P, Baalbaki M, Sandoval M, Hart D, Clay H, Coughlin S, Lagna G, Bayrak-Toydemir P, Hata A.

Sci Signal. 2018 Jan 16;11(513). pii: eaan6831. doi: 10.1126/scisignal.aan6831.


Let-7 microRNA-dependent control of leukotriene signaling regulates the transition of hematopoietic niche in mice.

Jiang X, Hawkins JS, Lee J, Lizama CO, Bos FL, Zape JP, Ghatpande P, Peng Y, Louie J, Lagna G, Zovein AC, Hata A.

Nat Commun. 2017 Jul 25;8(1):128. doi: 10.1038/s41467-017-00137-y.


Hyperactive locomotion in a Drosophila model is a functional readout for the synaptic abnormalities underlying fragile X syndrome.

Kashima R, Redmond PL, Ghatpande P, Roy S, Kornberg TB, Hanke T, Knapp S, Lagna G, Hata A.

Sci Signal. 2017 May 2;10(477). pii: eaai8133. doi: 10.1126/scisignal.aai8133.


Laboratory testing protocol to identify critical factors in bacterial compliance monitoring.

Abbaszadegan M, Ghatpande P, Brereton J, Alum A, Narasimhan R.

Water Sci Technol. 2003;47(3):131-6.


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